N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

Base Information

Chemical Name:N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide
CAS No.:30961-30-9
Molecular Formula:C₂₄H₂₇N₅O₄S
Molecular Weight:481.575
Hs Code.:

Synonyms:N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

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Chemical Property of N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

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Technology Process of N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

There total 6 articles about N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 2015-16-9
N-(4-[2-amino-ethyl]-benzenesulfonyl)-N'-cyclohexyl urea

: C₁₂H₁₀N₂O₄

: 30961-30-9
N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

Guidance literature:: With triethylamine; In acetone; at 20 ℃; for 4h;
DOI:10.1515/znb-2020-0134

Reference yield:

: tert-butyl (4-(N-(cyclohexylcarbamoyl)sulfamoyl)phenethyl)carbamate

: 30961-30-9
N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

2: triethylamine / acetone / 4 h / 20 °C

With triethylamine; trifluoroacetic acid; In dichloromethane; acetone;
DOI:10.1515/znb-2020-0134

Reference yield:

: 258262-54-3
tert-butyl (4-sulfamoyl phenethyl)carbamate

: 30961-30-9
N-{4-[N-(cyclohexylcarbamoyl)sulfamoyl]phenethyl}quinoxaline-2-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / acetone / 1 h / Reflux

1.2: 6 h / Reflux

2.1: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

3.1: triethylamine / acetone / 4 h / 20 °C

With potassium carbonate; triethylamine; trifluoroacetic acid; In dichloromethane; acetone;
DOI:10.1515/znb-2020-0134